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Descriptor English: Albinism, Oculocutaneous
Descriptor Spanish: Albinismo Oculocutáneo
Descriptor albinismo oculocutáneo
Entry term(s) albinismo amarillo mutante
albinismo tirosinasa negativo
albinismo tirosinasa positivo
Scope note: Grupo heterogéneo de trastornos autosómicos recesivos que comprenden al menos cuatro tipos reconocidos, y todos tienen en comun diversos grados de hipopigmentación de la piel, pelo y ojos. Los dos más comunes son los tipos tirosinasa-positivo y tirosinasa negativo.
Descriptor Portuguese: Albinismo Oculocutâneo
Descriptor French: Albinisme oculocutané
Entry term(s): Albinism, Tyrosinase Negative
Albinism, Tyrosinase Positive
Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Positive
Albinism, Yellow Mutant
Albinism, Yellow-Mutant
Mutant Albinism, Yellow
Mutant Albinisms, Yellow
Oculocutaneous Albinism
Tyrosinase-Negative Albinism
Tyrosinase-Positive Albinism
Yellow Mutant Albinism
Yellow-Mutant Albinism
Tree number(s): C11.270.040.545
C16.320.290.040.100
C16.320.565.100.102.100
C16.320.850.080.100
C17.800.621.440.102.100
C17.800.827.080.100
C18.452.648.100.102.100
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D016115
Scope note: Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Albinism (1966-1990)
Public MeSH Note: 91
History Note: 91
DeCS ID: 28852
Unique ID: D016115
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1990/02/12
Revision Date: 2016/07/01
Albinism, Oculocutaneous - Preferred
Concept UI M0024616
Scope note Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.
Preferred term Albinism, Oculocutaneous
Entry term(s) Oculocutaneous Albinism
Albinism, Tyrosinase-Negative - Narrower
Concept UI M0024617
Preferred term Albinism, Tyrosinase-Negative
Entry term(s) Albinism, Tyrosinase Negative
Tyrosinase-Negative Albinism
Albinism, Tyrosinase-Positive - Narrower
Concept UI M0024618
Preferred term Albinism, Tyrosinase-Positive
Entry term(s) Albinism, Tyrosinase Positive
Tyrosinase-Positive Albinism
Albinism, Yellow-Mutant - Narrower
Concept UI M0024619
Preferred term Albinism, Yellow-Mutant
Entry term(s) Albinism, Yellow Mutant
Mutant Albinism, Yellow
Mutant Albinisms, Yellow
Yellow Mutant Albinism
Yellow-Mutant Albinism



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